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Sample GSM1556702 Query DataSets for GSM1556702
Status Public on Dec 15, 2014
Title SLE1
Sample type SRA
 
Source name fibroblast
Organism Homo sapiens
Characteristics genotype/variation: SLE
passages: passages 4-11
tissue: skin biopsies
Treatment protocol untreated
Growth protocol DMEM with 10% FCS
Extracted molecule total RNA
Extraction protocol Total RNA from fibroblasts was extracted with the RNeasy Mini Kit (Qiagen) followed by DNase I digestion.
RNA libraries were prepared for sequencing using standard Illumina protocols
Strand specific RNA-Seq (dUTP method)
 
Library strategy RNA-Seq
Library source transcriptomic
Library selection cDNA
Instrument model Illumina HiSeq 2500
 
Description L2245
Data processing For data analyses a splice junction library with a length of 120 nucleotides (60+60) per splice junction was created based on known exon-exon junctions according to the Ensembl Genes annotation (v. 67, May 2012)
Alignment of the reads to the hg19 transcriptome was performed with pBWA
A counts-per-gene table was created based on the overlap of the uniquely mapped reads with the Ensembl Genes annotation for hg19, using BEDtools (v. 2.11)
RPKM (reads per kilobase per million reads) values were calculated based on the raw read counts and used as a measure of absolute expression levels.
Genome_build: hg19
Supplementary_files_format_and_content: excel file with RPKM counts table
 
Submission date Dec 01, 2014
Last update date May 15, 2019
Contact name Min Ae Lee-Kirsch
E-mail(s) MinAe.Lee-Kirsch@uniklinikum-dresden.de
Organization name TU Dresden
Department Universitätsklinikum Carl Gustav Carus
Lab Molekulare Pädiatrie
Street address Fetscherstraße 74
City Dresden
ZIP/Postal code 01307
Country Germany
 
Platform ID GPL16791
Series (1)
GSE63755 Defective removal of ribonucleotides from DNA promotes systemic autoimmunity
Relations
BioSample SAMN03247270
SRA SRX791744

Supplementary data files not provided
SRA Run SelectorHelp
Raw data are available in SRA
Processed data are available on Series record

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